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Disorder of magnesium transport

MONDO:0017765

An inherited metabolic disease that is has its basis in the disruption of magnesium ion transport.

Also known as: inborn error of magnesium ion transport, inborn magnesium ion transport disorder, rare inborn error of magnesium ion transport

28 clinical trials for this condition and its sub-types.

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Sub-types

Familial primary hypomagnesemia (4) EGF-related primary hypomagnesemia with intellectual disability (0) Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (0) Familial primary hypomagnesemia with hypocalcuria (0) Familial primary hypomagnesemia with normocalciuria and normocalcemia (0) Familial primary hypomagnesemia with normocalcuria (0) Hypomagnesemia 7, renal, with or without dilated cardiomyopathy (0) Hypomagnesemia, seizures, and intellectual disability (0) Hypomagnesemia, seizures, and intellectual disability 1 (0) Hypomagnesemia, seizures, and intellectual disability 2 (0) Intestinal hypomagnesemia 1 (0) Isolated autosomal dominant hypomagnesemia, Glaudemans type (0) Renal hypomagnesemia 2 (0) Renal hypomagnesemia 3 (0) Renal hypomagnesemia 4 (0) Renal hypomagnesemia 5 with ocular involvement (0) Renal hypomagnesemia 6 (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inborn errors of metabolism (42) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of metabolite absorption and transport (0) Disorder of mineral absorption and transport (0)
Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 5 Completed 7
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